dc.contributor.author |
Kwenda, Stanford
|
|
dc.contributor.author |
Gorshkov, Vladimir
|
|
dc.contributor.author |
Ramesh, Aadi Moolam
|
|
dc.contributor.author |
Naidoo, Sanushka
|
|
dc.contributor.author |
Rubagotti, Enrico
|
|
dc.contributor.author |
Birch, Paul R. J.
|
|
dc.contributor.author |
Moleleki, Lucy N.
|
|
dc.date.accessioned |
2016-05-06T16:02:35Z |
|
dc.date.available |
2016-05-06T16:02:35Z |
|
dc.date.issued |
2016-01-12 |
|
dc.description |
Additional file 1: Table S1. Complete list of RNA-seq detected sRNAs
(XLSX 19 kb) |
en_ZA |
dc.description |
Additional file 2: Table S2. Predicted transcription start sites of RNA-seq
detected sRNAs (XLSX 9114 kb) |
en_ZA |
dc.description |
Additional file 3: Table S3. List of in silico predicted sRNAs using RITs
from WebGester DB. S2A: Forward strand predictions. S2B: Complementary
strand predictions (XLSX 30 kb) |
en_ZA |
dc.description |
Additional file 4: Table S4. Combined list of predicted sRNA using
SIPHT and RITs from WebGester DB. S3A: Matches of in silico predictions
with SIPHT (forward strand) S3B: Matches of in silico predictions with
SIPHT (complementary strand) (XLSX 15 kb) |
en_ZA |
dc.description |
Additional file 5: Table S5. Conservation analysis in Soft Rot
Enterobacteriaceae (XLSX 16 kb) |
en_ZA |
dc.description |
Additional file 6: Table S6. Confirmation of RT-PCR amplicons by
sequencing and BLASTn against respective sRNA sequences (XLSX 9 kb) |
en_ZA |
dc.description |
Additional file 7: Table S7. Differentially expressed sRNA under
nutrient-rich and starvation conditions (XLSX 19 kb) |
en_ZA |
dc.description |
Additional file 8: Table S8. List of primers used for RT-PCR validation
of novel sRNAs (DOCX 12 kb) |
en_ZA |
dc.description |
Additional file 9: Table S9. List of primers used for RT-qPCR validation
of RNA-seq expression data (DOCX 12 kb) |
en_ZA |
dc.description.abstract |
BACKGROUND : Small RNAs (sRNAs) have emerged as important regulatory molecules and have been studied in
several bacteria. However, to date, there have been no whole-transcriptome studies on sRNAs in any of the Soft Rot
Enterobacteriaceae (SRE) group of pathogens. Although the main ecological niches for these pathogens are plants, a
significant part of their life cycle is undertaken outside their host within adverse soil environment. However, the
mechanisms of SRE adaptation to this harsh nutrient-deficient environment are poorly understood.
RESULTS : In the study reported herein, by using strand-specific RNA-seq analysis and in silico sRNA predictions, we
describe the sRNA pool of Pectobacterium atrosepticum and reveal numerous sRNA candidates, including those that
are induced during starvation-activated stress responses. Consequently, strand-specific RNA-seq enabled detection
of 137 sRNAs and sRNA candidates under starvation conditions; 25 of these sRNAs were predicted for this bacterium in
silico. Functional annotations were computationally assigned to 68 sRNAs. The expression of sRNAs in P. atrosepticum
was compared under growth-promoting and starvation conditions: 68 sRNAs were differentially expressed with 47
sRNAs up-regulated under nutrient-deficient conditions. Conservation analysis using BLAST showed that most of the
identified sRNAs are conserved within the SRE. Subsequently, we identified 9 novel sRNAs within the P. atrosepticum
genome.
CONCLUSIONS : Since many of the identified sRNAs are starvation-induced, the results of our study suggests that sRNAs
play key roles in bacterial adaptive response. Finally, this work provides a basis for future experimental characterization
and validation of sRNAs in plant pathogens. |
en_ZA |
dc.description.department |
Forestry and Agricultural Biotechnology Institute (FABI) |
en_ZA |
dc.description.department |
Microbiology and Plant Pathology |
en_ZA |
dc.description.librarian |
am2016 |
en_ZA |
dc.description.sponsorship |
The National Research
Foundation (NRF) Thuthuka Grant UID: 69362; UID BFG 93685 and NRF South
Africa Russia Bilateral Grant UID: 75252 and from the Russian Foundation for
Basic Research (Research Project No. 15-04-02380). The University of Pretoria
is acknowledged for providing a studentship for S. Kwenda. V. Gorshkov is
supported by The Russian Science Foundation (Project No. 15-14-10022). |
en_ZA |
dc.description.uri |
http://www.biomedcentral.com/bmcgenomics |
en_ZA |
dc.identifier.citation |
Kwenda, S, Gorshkov, V, Ramesh, AM, Naidoo, S, Rubagotti E, Birch, PRJ & Moleleki, LN 2016, 'Discovery and profiling of small RNAs responsive to stress conditions in the plant pathogen Pectobacterium atrosepticum', BMC Genomics, 17, art. #47, pp. 1-15. |
en_ZA |
dc.identifier.issn |
1471-2164 |
|
dc.identifier.other |
10.1186/s12864-016-2376-0 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/52530 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
BioMed Central |
en_ZA |
dc.rights |
© 2016 Kwenda et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License. |
en_ZA |
dc.subject |
Strand-specific RNA-seq |
en_ZA |
dc.subject |
Pectobacterium atrosepticum |
en_ZA |
dc.subject |
In silico prediction |
en_ZA |
dc.subject |
Transcriptome |
en_ZA |
dc.subject |
Riboswitches |
en_ZA |
dc.subject |
5′ UTR |
en_ZA |
dc.subject |
3′ UTR |
en_ZA |
dc.subject |
Small RNAs (sRNAs) |
en_ZA |
dc.subject |
Soft Rot Enterobacteriaceae (SRE) |
en_ZA |
dc.title |
Discovery and profiling of small RNAs responsive to stress conditions in the plant pathogen Pectobacterium atrosepticum |
en_ZA |
dc.type |
Article |
en_ZA |